Canonical Allele Identifier: CA218400668
Gene: KCNJ11 HGNC NCBI

Linked Data

dbSNP Id: rs926158416

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388326_17388328del , CM000673.2:g.17388326_17388328del GRCh38
NC_000011.9:g.17409873_17409875del , CM000673.1:g.17409873_17409875del GRCh37
NC_000011.8:g.17366449_17366451del NCBI36
NG_012446.1:g.5333_5335del

Transcript Alleles

HGVS Amino-acid Change
ENST00000528992.2:c.-213-251_-213-249del ENSP00000436479.2:n.-213-251_-213-249del
ENST00000682350.1:c.-16-481_-16-479del ENSP00000508090.1:n.-16-481_-16-479del
ENST00000682764.1:c.-16-481_-16-479del ENSP00000506780.1:n.-16-481_-16-479del
ENST00000339994.5:c.-236_-234del MANE Select ENSP00000345708.4:n.-236_-234del
ENST00000339994.4:c.-236_-234del ENSP00000345708.4:n.-236_-234del
ENST00000526912.1:c.-75-251_-75-249del ENSP00000432729.1:n.-75-251_-75-249del
ENST00000528731.1:c.-16-481_-16-479del ENSP00000434755.1:n.-16-481_-16-479del
ENST00000528992.1:c.33-251_33-249del
NM_000525.3:c.-236_-234del NP_000516.3:n.-236_-234del
NM_001166290.1:c.-16-481_-16-479del NP_001159762.1:n.-16-481_-16-479del
XM_006718226.2:c.-16-481_-16-479del XP_006718289.1:n.-16-481_-16-479del
XM_006718226.3:c.-16-481_-16-479del XP_006718289.1:n.-16-481_-16-479del
XM_017017680.1:c.-16-481_-16-479del XP_016873169.1:n.-16-481_-16-479del
NM_001166290.2:c.-16-481_-16-479del NP_001159762.1:n.-16-481_-16-479del
NM_001377296.1:c.-75-251_-75-249del NP_001364225.1:n.-75-251_-75-249del
NM_001377297.1:c.-16-481_-16-479del NP_001364226.1:n.-16-481_-16-479del
NM_000525.4:c.-236_-234del MANE Select NP_000516.3:n.-236_-234del